Cargando…
Integrative analyses shed new light on human ribosomal protein gene regulation
Ribosomal protein genes (RPGs) are important house-keeping genes that are well-known for their coordinated expression. Previous studies on RPGs are largely limited to their promoter regions. Recent high-throughput studies provide an unprecedented opportunity to study how human RPGs are transcription...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921865/ https://www.ncbi.nlm.nih.gov/pubmed/27346035 http://dx.doi.org/10.1038/srep28619 |
_version_ | 1782439551081381888 |
---|---|
author | Li, Xin Zheng, Yiyu Hu, Haiyan Li, Xiaoman |
author_facet | Li, Xin Zheng, Yiyu Hu, Haiyan Li, Xiaoman |
author_sort | Li, Xin |
collection | PubMed |
description | Ribosomal protein genes (RPGs) are important house-keeping genes that are well-known for their coordinated expression. Previous studies on RPGs are largely limited to their promoter regions. Recent high-throughput studies provide an unprecedented opportunity to study how human RPGs are transcriptionally modulated and how such transcriptional regulation may contribute to the coordinate gene expression in various tissues and cell types. By analyzing the DNase I hypersensitive sites under 349 experimental conditions, we predicted 217 RPG regulatory regions in the human genome. More than 86.6% of these computationally predicted regulatory regions were partially corroborated by independent experimental measurements. Motif analyses on these predicted regulatory regions identified 31 DNA motifs, including 57.1% of experimentally validated motifs in literature that regulate RPGs. Interestingly, we observed that the majority of the predicted motifs were shared by the predicted distal and proximal regulatory regions of the same RPGs, a likely general mechanism for enhancer-promoter interactions. We also found that RPGs may be differently regulated in different cells, indicating that condition-specific RPG regulatory regions still need to be discovered and investigated. Our study advances the understanding of how RPGs are coordinately modulated, which sheds light to the general principles of gene transcriptional regulation in mammals. |
format | Online Article Text |
id | pubmed-4921865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49218652016-06-28 Integrative analyses shed new light on human ribosomal protein gene regulation Li, Xin Zheng, Yiyu Hu, Haiyan Li, Xiaoman Sci Rep Article Ribosomal protein genes (RPGs) are important house-keeping genes that are well-known for their coordinated expression. Previous studies on RPGs are largely limited to their promoter regions. Recent high-throughput studies provide an unprecedented opportunity to study how human RPGs are transcriptionally modulated and how such transcriptional regulation may contribute to the coordinate gene expression in various tissues and cell types. By analyzing the DNase I hypersensitive sites under 349 experimental conditions, we predicted 217 RPG regulatory regions in the human genome. More than 86.6% of these computationally predicted regulatory regions were partially corroborated by independent experimental measurements. Motif analyses on these predicted regulatory regions identified 31 DNA motifs, including 57.1% of experimentally validated motifs in literature that regulate RPGs. Interestingly, we observed that the majority of the predicted motifs were shared by the predicted distal and proximal regulatory regions of the same RPGs, a likely general mechanism for enhancer-promoter interactions. We also found that RPGs may be differently regulated in different cells, indicating that condition-specific RPG regulatory regions still need to be discovered and investigated. Our study advances the understanding of how RPGs are coordinately modulated, which sheds light to the general principles of gene transcriptional regulation in mammals. Nature Publishing Group 2016-06-27 /pmc/articles/PMC4921865/ /pubmed/27346035 http://dx.doi.org/10.1038/srep28619 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Li, Xin Zheng, Yiyu Hu, Haiyan Li, Xiaoman Integrative analyses shed new light on human ribosomal protein gene regulation |
title | Integrative analyses shed new light on human ribosomal protein gene regulation |
title_full | Integrative analyses shed new light on human ribosomal protein gene regulation |
title_fullStr | Integrative analyses shed new light on human ribosomal protein gene regulation |
title_full_unstemmed | Integrative analyses shed new light on human ribosomal protein gene regulation |
title_short | Integrative analyses shed new light on human ribosomal protein gene regulation |
title_sort | integrative analyses shed new light on human ribosomal protein gene regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921865/ https://www.ncbi.nlm.nih.gov/pubmed/27346035 http://dx.doi.org/10.1038/srep28619 |
work_keys_str_mv | AT lixin integrativeanalysesshednewlightonhumanribosomalproteingeneregulation AT zhengyiyu integrativeanalysesshednewlightonhumanribosomalproteingeneregulation AT huhaiyan integrativeanalysesshednewlightonhumanribosomalproteingeneregulation AT lixiaoman integrativeanalysesshednewlightonhumanribosomalproteingeneregulation |